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ROBITUSSIN CF SYRUP - SFDA Drug Approval Details
Approvals
/
SFDA
/
ROBITUSSIN CF SYRUP
Authorized
NCE
ROBITUSSIN CF SYRUP
Unknown
🇸🇦 Saudi Food and Drug Authority
Approval Date
N/A
Approval ID
87ad8e2d5f84eff7
Company
Unknown
Type
NCE
Approval Details
Approval Id
87ad8e2d5f84eff7
Drug Approval Sfda Name
ROBITUSSIN CF SYRUP
Trade Name
ROBITUSSIN CF SYRUP
Generic Name
GUAIFENESIN,PSEUDOEPHEDRINE HYDROCHLORIDE,DEXTROMETHORPHAN
Register Number
1-5412-19
Register Year
2019
Drug Type
NCE
Route Of Administration
Oral use
Package Type
Bottle
Package Size
1
Size
118
Size Unit
ml
Legal Status
Prescription
Authorization Status
Valid
Marketing Status
Marketed
Product Control
Uncontrolled
Storage Conditions
store below 25°c
Shelf Life
24 Months
Distribution Site
Pharmacy
Description Code
21000002038-140-100000073652
Price
8.8
Active Ingredients
Authorized
Quick Info
Agency
SFDA
Country
🇸🇦
Approval ID
87ad8e2d5f84eff7
Type
NCE
Back to SFDA Approvals